Reversed-phase TLC study of the lipophilicity of fourteen 1,3-benzoxazol-2(3H)-one derivatives and comparison with isomeric 1,2-benzisoxazol-3(2H)-one analogs-Reference-Cited by-同舟云学术

Reversed-phase TLC study of the lipophilicity of fourteen 1,3-benzoxazol-2(3H)-one derivatives and comparison with isomeric 1,2-benzisoxazol-3(2H)-one analogs

Published:2011-08 Issue:4 Volume:24 Page:348-351
ISSN:0933-4173
Container-title:Journal of Planar Chromatography – Modern TLC
language:en
Short-container-title:Journal of Planar Chromatography – Modern TLC

Author:

Skibiński Robert,Sławik Tomasz,Kaczkowska Martyna

Publisher

Akademiai Kiado Zrt.

Subject

Clinical Biochemistry,Biochemistry,Analytical Chemistry

Link

https://www.akademiai.com/doi/pdf/10.1556/jpc.24.2011.4.14

Reference15 articles.

1. RP TLC Determination of the Lipophilicity of New 10‐Substituted 2,7‐Diazaphenothiazines*

2. Determination of the lipophilicity of selected isoquinoline alkaloids by RP-TLC

3. LC and Principal Component Analysis in the Lipophilicity Study of Seven Angiotensin II-AT1 Receptor Antagonists (Sartans)

4. Estimating the lipophilicity of a number of 2-amino-1-cyclohexanol derivatives exhibiting anticonvulsant activity

5. RP-TLC determination of the lipophilicity of 1-substituted pyrrolidin-2-one derivatives. Correlation of lipophilicity with affinity for α-adrenoceptors

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Lipophilicity of New Anticancer 1,6- and 3,6-diazaphenothiazines by of Use RP TLC and Different Computational Methods†;Journal of Chromatographic Science;2018-02-07

2. Estimation of the Lipophilicity of New Anticancer and Immunosuppressive 1,8-Diazaphenothiazine Derivatives;Journal of Chromatographic Science;2014-06-30

3. Revisiting thin-layer chromatography as a lipophilicity determination tool. Part IV — A closer look on extrapolation and averaging;Acta Chromatographica;2014-03

4. High Performance Thin-Layer Chromatography;Green Chromatographic Techniques;2013-11-13

5. A TLC Study of the lipophilicity of thirty-two acetylcholinesterase inhibitors — 1,2,3,4-tetrahydroacridine and 2,3-dihydro-1H-cyclopenta[b]quinoline derivatives;Open Chemistry;2013-06-01